WO2011128295A1 - Thienodithiinderivate als fungizide - Google Patents
Thienodithiinderivate als fungizide Download PDFInfo
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- WO2011128295A1 WO2011128295A1 PCT/EP2011/055635 EP2011055635W WO2011128295A1 WO 2011128295 A1 WO2011128295 A1 WO 2011128295A1 EP 2011055635 W EP2011055635 W EP 2011055635W WO 2011128295 A1 WO2011128295 A1 WO 2011128295A1
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- 0 *c([s]1)cc2c1SC(S(*)=O)=C(*)S2(=O)=O Chemical compound *c([s]1)cc2c1SC(S(*)=O)=C(*)S2(=O)=O 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
Definitions
- the present invention relates to the novel thienodithiin derivatives, processes for their preparation, their use for controlling undesirable microorganisms, in particular phytopathogenic fungi, in crop protection, in the household and hygiene sector and in the protection of materials, and pesticides containing these thienodithiin derivatives.
- the present invention now relates to novel thienodithiin derivatives of the general formula (I)
- R 1 is halogen
- n 0, 1 or 2
- R 2 is hydrogen, cyano or aminocarbonyl
- R 3 is optionally mono- or polysubstituted by halogen-substituted Ci-Ci2-alkyl, in each case optionally mono- or polysubstituted by halogen, Ci-C i-alkyl or Ci-C i -haloalkyl-substituted aryl, aryl- (Ci-C 4 -alkyl) , Hetaryl or hetaryl (Ci-C 4 alkyl).
- Thienodithiine derivatives of the formula (I) according to the invention are very suitable for controlling unwanted microorganisms, in particular phytopathogenic fungi.
- the abovementioned compounds according to the invention can be used both in crop protection, in the area of household and hygiene as well as in the protection of materials.
- thienodithiine derivatives of the invention are generally defined by the formula (I).
- Preferred thienodithiine derivatives of the formula (I) are those in which the radicals have the following meanings. These preferred meanings apply equally to the intermediates in the preparation of compounds of the formula (I).
- R 1 is preferably fluorine, chlorine or bromine.
- R 1 particularly preferably represents fluorine or chlorine.
- R 1 very particularly preferably represents chlorine.
- n is preferably 0 or 2.
- n is particularly preferably 0.
- n is also particularly preferred for 2.
- R is preferably cyano or aminocarbonyl.
- R 2 is particularly preferably cyano.
- R 2 is also particularly preferably aminocarbonyl.
- R 3 preferably represents optionally mono- or polysubstituted by fluorine, chlorine or bromine-substituted Ci-Cg-alkyl, in each case optionally mono- or polysubstituted by fluorine, chlorine, bromine, trifluoromethyl, substituted phenyl, phenyl (Ci-C 4 alkyl Hetaryl or hetaryl- (C 1 -C 4 -alkyl), wherein Hetaryl is selected from pyridinyl, pyrimidinyl, pyrazinyl, pyridazinyl, furyl, thienyl, pyrrole, pyrazole, imidazole.
- R 3 is particularly preferably in each case optionally mono- or polysubstituted by fluorine, chlorine or bromine-substituted methyl, ethyl, n-propyl, isopropyl, n-, i-, s- or t-butyl, hexyl or octyl, in each case optionally mono- or polysubstituted by fluorine, chlorine, bromine, trifluoromethyl, substituted phenyl, benzyl, 1-phenethyl, 2-phenenthyl, pyridinyl or pyridinylmethyl.
- R 3 very particularly preferably represents methyl, ethyl, n-propyl, n-butyl, n-hexyl or n-octyl, in each case optionally substituted by chlorine, in each case optionally mono- or polysubstituted by fluorine or chlorine, phenyl, benzyl, 3-pyridinyl , 2-pyridinyl or 4-pyridinyl.
- the thienodithiine derivatives which can be used according to the invention may optionally be used as mixtures of various possible isomeric forms, in particular of stereoisomers, such as, for example, B. E and Z, threo and erythro, and optical isomers, but optionally also of tautomers. It is claimed both the E and the Z isomers, as well as the threo and erythro, and the optical isomers, any mixtures of these isomers, as well as the possible tautomeric forms.
- Thienodithiine derivatives of the formula (I) can be prepared, for example, according to the following scheme:
- the present invention further relates to a crop protection agent for controlling undesirable fungi comprising at least one of the thienodithiine derivatives of the formula (I).
- a crop protection agent for controlling undesirable fungi comprising at least one of the thienodithiine derivatives of the formula (I).
- Preference is given to fungicidal compositions which contain agricultural auxiliaries, solvents, carriers, surface-active substances or extenders.
- the invention relates to a method for controlling unwanted microorganisms, characterized in that according to the invention thienodithiin derivatives of the formula (I) on the phytopathogenic fungi and / or their habitat organizingstingt.
- the carrier means a natural or synthetic, organic or inorganic substance with which the active ingredients for better applicability, v. A. for planting or plant parts or seeds, mixed or connected.
- the carrier which may be solid or liquid, is generally inert and should be useful in agriculture.
- Suitable solid or liquid carriers are: e.g. Ammonium salts and ground natural minerals, such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as fumed silica, alumina and natural or synthetic silicates, resins, waxes, solid fertilizers, water, alcohols, especially Butanol, organic solvents, mineral and vegetable oils and derivatives thereof. Mixtures of such carriers can also be used.
- Suitable solid carriers for granules are: e.g.
- Cracked and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours, and granules of organic material such as sawdust, coconut shells, corn cobs and tobacco stems.
- Suitable liquefied gaseous diluents or carriers are those liquids which are gaseous at normal temperature and under atmospheric pressure, for example aerosol propellants, such as halogenated hydrocarbons, as well as butane, propane, nitrogen and carbon dioxide.
- Adhesives such as carboxymethyl cellulose, natural and synthetic powdery, granular or latex-shaped polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and natural phospholipids such as cephalins and lecithins, and synthetic phospholipids may be used in the formulations.
- Other additives may be mineral and vegetable oils.
- organic solvents can also be used as auxiliary solvents.
- Suitable liquid solvents are essentially: aromatics, such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons, such as chlorobenzenes, chloroethylenes or dichloromethane, aliphatic hydrocarbons, such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols , such as butanol or glycol and their ethers and esters, ketones, such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
- aromatics such as xylene, toluene or alkylnaphthalenes
- chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or dichloromethane
- the agents of the invention may additionally contain other ingredients, e.g. surfactants.
- Suitable surface-active substances are emulsifying and / or foam-forming agents, dispersants or wetting agents having ionic or nonionic properties or mixtures of these surface-active substances.
- Examples thereof are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphonic acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic acid esters, taurine derivatives (preferably alkyltaurates ), Phosphoric acid esters of polyethoxylated alcohols or phenols, fatty acid esters of polyols, and derivatives of the compounds containing sulphates, sulphonates and phosphates, eg Alkylaryl polyglycol ethers, alkylsulfonates, alkyl sulfates, arylsulfonates, protein hydrolysates, liginine sulfite waste liquors and methylcellulose.
- a surfactant is necessary when one of the active ingredients and / or one of the inert carriers is not soluble in water and when applied in water.
- the proportion of surface-active substances is between 5 and 40 percent by weight of the agent according to the invention.
- Dyes such as inorganic pigments, e.g. Iron oxide, titanium oxide, ferrocyan blue and organic dyes such as alizarin, azo and metal phthalocyanine dyes and trace nutrients such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
- additional components may also be included, e.g. protective colloids, binders, adhesives, thickeners, thixotropic substances, penetration enhancers, stabilizers, sequestering agents, complexing agents.
- the active ingredients can be combined with any solid or liquid additive commonly used for formulation purposes.
- the formulations generally contain from 0.05 to 99 wt .-%, 0.01 and 98 wt .-%, preferably between 0.1 and 95 wt .-%, particularly preferably between 0.5 and 90% active ingredient, completely more preferably between 10 and 70 weight percent.
- the active compounds or compositions according to the invention can be used as such or as a function of their physical and / or chemical properties in the form of their formulations or the use forms prepared therefrom, such as aerosols, capsule suspensions, cold mist concentrates, hot mist concentrates, encapsulated granules, fine granules, flowable concentrates for the treatment of seed, ready-to-use solutions, dustable powders, emulsifiable concentrates, oil-in-water emulsions, water-in-oil emulsions, macrogranules, microgranules, oil-dispersible powders, oil-miscible flowable concentrates, oil-miscible liquids, Foams, pastes, pesticide-coated seeds, suspension concentrates, suspension-emulsion concentrates, soluble concentrates, suspensions, wettable powders, soluble powders, dusts and granules, water-soluble granules or tablets, water-soluble powders for seed treatment, wett
- the formulations mentioned can be prepared in a manner known per se, e.g. by mixing the active compounds with at least one customary diluent, solvent or diluent, emulsifier, dispersing and / or binding or fixing agent, wetting agent, water repellent, optionally siccatives and UV stabilizers and optionally dyes and pigments, defoaming agents, preservatives, secondary thickeners, adhesives, gibberellins and other processing aids.
- compositions according to the invention comprise not only formulations which are already ready for use and which can be applied to the plant or the seed with a suitable apparatus, but also commercial concentrates which have to be diluted with water before use.
- the active compounds according to the invention as such or in their (commercial) formulations and in the formulations prepared from these formulations in admixture with other (known) agents such as insecticides, attractants, sterilants, bactericides, acaricides, nematicides, fungicides, growth regulators, herbicides, fertilizers , Safeners or semiochemicals.
- the treatment according to the invention of the plants and plant parts with the active ingredients or agents is carried out directly or by acting on their environment, habitat or storage space according to the usual treatment methods, e.g. by dipping, spraying, spraying, sprinkling, vaporizing, atomizing, atomizing, sprinkling, foaming, brushing, spreading, pouring, drip irrigation and in the case of propagation material, in particular in the case of seeds Furthermore, by dry pickling, wet pickling, slurry pickling, encrusting, single or multi-layer wrapping etc. It is also possible to apply the active ingredients by the ultra-low-volume method or to inject the active ingredient preparation or the active ingredient itself into the soil.
- the invention further comprises a method of treating seed.
- the invention further relates to seed which has been treated according to one of the methods described in the previous paragraph.
- the seeds of the invention are used in seed protection processes unwanted mushrooms.
- a seed treated with at least one active ingredient according to the invention is used.
- the active compounds or compositions according to the invention are also suitable for the treatment of seed.
- Much of the damage to crop plants caused by harmful organisms is caused by infestation of the seed during storage or after sowing and during and after germination of the plant. This phase is particularly critical because the roots and shoots of the growing plant are particularly sensitive and may cause only a small damage to the death of the plant. There is therefore a great interest in protecting the seed and the germinating plant by using suitable means.
- the present invention therefore also relates to a method of protecting seed and germinating plants from the infestation of phytopathogenic fungi by treating the seed with an agent according to the invention.
- the invention also relates to the use of the seed treatment agents of the invention for protecting the seed and the germinating plant from phytopathogenic fungi.
- the invention relates to seed which has been treated for protection against phytopathogenic fungi with an agent according to the invention.
- the active compounds or agents according to the invention can also be used in particular in the case of transgenic seed, wherein the plant growing from this seed is capable of expressing a protein which acts against pests.
- the active compounds or agents according to the invention By treating such seeds with the active compounds or agents according to the invention, it is possible to combat pests already determined by the expression of, for example, insecticidal protein.
- a further synergistic effect can be observed, which additionally increases the effectiveness for protection against pest infestation.
- compositions according to the invention are suitable for the protection of seed of any plant variety used in agriculture, in the greenhouse, in forests or in horticulture and viticulture.
- these are seeds of cereals (such as wheat, barley, rye, triticale, millet and oats), corn, cotton, soya, rice, potatoes, sunflower, bean, coffee, turnip (eg sugar beet and fodder beet), peanut, Rapeseed, poppy, olive, coconut, cocoa, sugarcane, tobacco, vegetables (such as tomato, cucumber, onions and lettuce), turf and ornamental plants (see also below).
- cereals such as wheat, barley, rye, triticale and oats
- corn and rice are seeds of cereals (such as wheat, barley, rye, triticale, millet and oats), corn, cotton, soya, rice, potatoes, sunflower, bean, coffee, turnip (eg sugar beet and fodder beet), peanut, Rapeseed,
- transgenic seed As also described below, the treatment of transgenic seed with the active substances or agents according to the invention is of particular importance.
- the heterologous gene in transgenic seed may e.g. come from microorganisms of the species Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium.
- this heterologous gene is derived from Bacillus sp., Wherein the gene product has an activity against the European corn borer and / or Western Com Rootworm.
- the heterologous gene is particularly preferably derived from Bacillus thurin giensis.
- the agent according to the invention is applied to the seed alone or in a suitable formulation.
- the seed is treated in a condition that is so stable that no damage occurs during the treatment.
- the treatment of the seed can be done at any time between harvesting and sowing.
- seed is used which has been separated from the plant and freed from flasks, shells, stems, hull, wool or pulp.
- seed may be used which has been harvested, cleaned and dried to a moisture content of below 15% by weight.
- seed may also be used which, after drying, e.g. treated with water and then dried again.
- the agents according to the invention can be applied directly, ie without containing further components and without being diluted. As a rule, it is preferable to use the appropriations in the form of an appropriate form lation on the seed. Suitable formulations and methods for seed treatment are known to those skilled in the art and are described, for example, in the following documents: US 4,272,417 A, US 4,245,432 A, US 4,808,430 A, US 5,876,739 A, US 2003/0176428 Al, WO 2002/080675 Al, WO 2002 / 028186 A2.
- the active compounds which can be used according to the invention can be converted into the customary seed dressing formulations, such as solutions, emulsions, suspensions, powders, foams, slurries or other seed coating compositions, as well as ULV formulations.
- formulations are prepared in a known manner by mixing the active ingredients with conventional additives, such as conventional extenders and solvents or diluents, dyes, wetting agents, dispersants, emulsifiers, defoamers, preservatives, secondary thickeners, adhesives, gibberellins and water.
- conventional additives such as conventional extenders and solvents or diluents, dyes, wetting agents, dispersants, emulsifiers, defoamers, preservatives, secondary thickeners, adhesives, gibberellins and water.
- Dyes which may be present in the seed dressing formulations which can be used according to the invention are all dyes customary for such purposes. Both water-insoluble pigments and water-soluble dyes are useful in this case. Examples which may be mentioned under the names rhodamine B, C.I. Pigment Red 112 and C.I. Solvent Red 1 known dyes.
- Suitable wetting agents which may be present in the seed dressing formulations which can be used according to the invention are all wetting-promoting substances customary for the formulation of agrochemical active compounds.
- Preferably used are alkylnaphthalene sulfonates, such as diisopropyl or diisobutyl naphthalene sulfonates.
- Suitable dispersants and / or emulsifiers which may be present in the seed dressing formulations which can be used according to the invention are all nonionic, anionic and cationic dispersants customary for the formulation of agrochemical active compounds.
- Preferably usable are nonionic or anionic dispersants or mixtures of nonionic or anionic dispersants.
- Particularly suitable nonionic dispersants are, in particular, ethylene oxide-propylene oxide, block polymers, alkylphenol polyglycol ethers and tristryrylphenol polyglycol ethers and their phosphated or sulfated derivatives.
- Suitable anionic dispersants are, in particular, lignosulfonates, polyacrylic acid salts and arylsulfonate-formaldehyde condensates.
- Defoamers which may be present in the seed dressing formulations which can be used according to the invention are all foam-inhibiting substances customary for the formulation of agrochemical active compounds.
- Preferably usable are silicone defoamers and magnesium stearate.
- Preservatives which may be present in the seed dressing formulations which can be used according to the invention are all substances which can be used for such purposes in agrochemical compositions. Examples which may be mentioned are dichlo- rophene and benzyl alcohol hemiformal.
- Suitable secondary thickeners which may be present in the seed dressing formulations which can be used according to the invention are all substances which can be used for such purposes in agrochemical compositions.
- Suitable adhesives which may be present in the seed dressing formulations which can be used according to the invention are all customary binders which can be used in pickling agents.
- Preferably mentioned are polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and Tylose.
- the gibberellins are known (see R. Wegler "Chemie der convinced- und Sch ingsbehimungsstoff", Vol. 2, Springer Verlag, 1970, pp. 401-412).
- the seed dressing formulations which can be used according to the invention can be used either directly or after prior dilution with water for the treatment of seed of various kinds, including seed of transgenic plants.
- additional synergistic effects may occur in interaction with the substances formed by expression.
- the seed dressing formulations which can be used according to the invention or the preparations prepared therefrom by the addition of water
- all mixing devices customarily usable for the dressing can be considered.
- the seed is placed in a mixer which adds either desired amount of seed dressing formulations, either as such or after prior dilution with water, and mixes until uniformly distributing the formulation on the seed .
- a drying process follows.
- the active compounds or compositions according to the invention have a strong fungicidal action and can be used for controlling unwanted fungi in crop protection and in the protection of materials.
- the thienodithiin derivatives according to the invention can be employed in crop protection for controlling Plasmodiophosphomycetes, Oomycetes, Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes.
- the fungicidal compositions according to the invention can be used curatively or protectively for controlling phytopathogenic fungi.
- the invention therefore also relates to curative and protective methods for controlling phytopathogenic fungi by the use of the active compounds or agents according to the invention, which are applied to the seed, the plant or plant parts, the fruits or the soil in which the plants grow.
- compositions according to the invention for controlling phytopathogenic fungi in plant protection comprise an effective but non-phytotoxic amount of the active compounds according to the invention.
- Effective but not phytotoxic amount means an amount of the agent of the invention sufficient to control or completely kill fungal disease of the plant and at the same time not cause any significant phytotoxicity symptoms. This rate of application may generally vary widely from a number of factors, for example the fungus to be controlled, the plant, the climatic conditions and the ingredients of the agents according to the invention.
- the good plant tolerance of the active ingredients in the necessary concentrations for controlling plant diseases allows treatment of aboveground plant parts, of plant and seed, and the soil.
- plants and parts of plants can be treated.
- plants are understood as meaning all plants and plant populations, such as desired and undesired wild plants or crop plants (including naturally occurring crop plants).
- Crop plants can be plants which can be obtained by conventional breeding and optimization methods or by biotechnological and genetic engineering methods or combinations of these methods, including the transgenic plants and including the plant varieties which can or can not be protected by plant breeders' rights.
- Plant parts are to be understood as meaning all aboveground and subterranean parts and organs of the plants, such as shoot, leaf, flower and root, examples of which include leaves, needles, stems, stems, flowers, fruiting bodies, fruits and seeds, and roots, tubers and rhizomes.
- the plant parts also include crops and vegetative and generative propagation material, such as cuttings, tubers, rhizomes, offshoots and seeds.
- the active compounds according to the invention are suitable for good plant tolerance, favorable toxicity to warm-blooded animals and good environmental compatibility for the protection of plants and plant organs, for increasing crop yields, improving the quality of the harvested crop. They can preferably be used as crop protection agents. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
- plants which can be treated according to the invention mention may be made of the following: cotton, flax, grapevine, fruits, vegetables, such as Rosaceae sp. (for example, pomegranates such as apple and pear, but also stone fruits such as apricots, cherries, almonds and peaches and soft fruits such as strawberries), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp. , Oleaceae sp., Actinidaceae sp., Lauraceae sp., Musaceae sp.
- Rosaceae sp. for example, pomegranates such as apple and pear, but also stone fruits such as apricots, cherries, almonds and peaches and soft fruits such as strawberries
- Rosaceae sp. for example, pomegranates such as apple and pear
- Rubiaceae sp. for example, coffee
- Theaceae sp. Sterculiceae sp.
- Rutaceae sp. for example, lemons, organs and grapefruit
- Solanaceae sp. for example tomatoes
- Liliaceae sp. Aster aceae sp.
- Umbelliferae sp. for example, Cruciferae sp., Chenopodiaceae sp., Cucurbitaceae sp. (for example cucumber), Alliaceae sp. leek, onion), Papilionaceae sp.
- Main crops such as Gramineae sp. (for example corn, turf, cereals such as wheat, rye, rice, barley, oats, millet and triticale), Poaceae sp. (eg sugarcane), Asteraceae sp. (for example sunflower), Brassicaceae sp. (for example, white cabbage, red cabbage, broccoli, cauliflower, Brussels sprouts, pak choi, kohlrabi, radishes and rapeseed, mustard, horseradish and cress), Fabacae sp. (for example, bean, peanuts), Papilionaceae sp. (for example, soybean), Solanaceae sp.
- plants and their parts can be treated.
- wild-type or plant species obtained by conventional biological breeding methods such as crossing or protoplast fusion
- plant cultivars and their parts are treated.
- transgenic plants and plant cultivars which have been obtained by genetic engineering if appropriate in combination with conventional methods (Genetically Modified Organisms), and parts thereof are treated.
- the term "parts” or “parts of plants” or “parts of plants” has been explained above, plants according to the invention are in each case treated with the plants which are commercially available or in use.Purple plants are understood as meaning plants with new properties ("traits"). which have been bred either by conventional breeding, by mutagenesis or by recombinant DNA techniques. These may be varieties, breeds, biotypes and genotypes.
- the treatment method of the invention may be used for the treatment of genetically modified organisms (GMOs), e.g. As plants or seeds are used.
- GMOs genetically modified organisms
- Genetically modified plants are plants in which a heterologous gene has been stably integrated into the genome.
- heterologous gene essentially refers to a gene that is provided or assembled outside the plant and that when introduced into the nuclear genome, chloroplast genome or mitochondrial genome imparts new or improved agronomic or other properties to the transformed plant Protein or polypeptide expressed or that it downregulates or shuts down another gene present in the plant or other genes present in the plant (for example by means of antisense technology, co-suppression technology or RNAi technology [RNA Interference]) ,
- a heterologous gene present in the genome is also referred to as a transgene.
- a transgene defined by its specific presence in the plant genome is referred to as a transformation or transgenic event.
- the treatment according to the invention can also lead to superadditive (“synergistic”) effects.
- the following effects are possible, which go beyond the expected effects: reduced application rates and / or extended spectrum of action and / or increased efficacy of the active ingredients and compositions that can be used according to the invention, better plant growth, increased tolerance to high or low Temperatures, increased tolerance to dryness or water or soil salinity, increased flowering, crop relief, ripening, higher yields, larger fruits, greater plant height, intense green color of the leaf, earlier flowering, higher quality and / or higher nutritional value of the harvested products, higher Sugar concentration in fruits, better shelf life and / or processability of harvested products.
- the active compound combinations according to the invention can also exert a strengthening effect on plants. They are therefore suitable for mobilizing the plant defense system against Attack by unwanted phytopathogenic fungi and / or microorganisms and / or viruses. This may optionally be one of the reasons for the increased effectiveness of the combinations according to the invention, for example against fungi.
- Plant-strengthening (resistance-inducing) substances in the present context should also mean those substances or substance combinations capable of stimulating the plant defense system in such a way that the treated plants, when subsequently inoculated with undesirable phytopathogenic fungi, have a considerable degree of resistance against have these undesirable phytopathogenic fungi.
- the substances according to the invention can therefore be employed for the protection of plants against attack by the mentioned pathogens within a certain period of time after the treatment.
- the period of time over which a protective effect is achieved generally extends from 1 to 10 days, preferably 1 to 7 days, after the treatment of the plants with the active substances.
- Plants and plant varieties which are preferably treated according to the invention include all plants which have genetic material conferring on these plants particularly advantageous, useful features (whether obtained by breeding and / or biotechnology).
- Plants and plant varieties which are also preferably treated according to the invention are resistant to one or more biotic stressors, i. These plants have an improved defense against animal and microbial pests such as nematodes, insects, mites, phytopathogenic fungi, bacteria, viruses and / or viroids.
- Plants and plant varieties which can also be treated according to the invention are those plants which are resistant to one or more abiotic stress factors.
- Abiotic stress conditions may include, for example, drought, cold and heat conditions, osmotic stress, waterlogging, increased soil salinity, increased exposure to minerals, ozone conditions, high light conditions, limited availability of nitrogen nutrients, limited availability of phosphorous nutrients, or avoidance of shade.
- Plants and plant varieties which can also be treated according to the invention are those plants which are characterized by increased yield properties.
- An increased yield can in these plants z. These include improved plant physiology, improved plant growth and improved plant development, such as water efficiency, water retention efficiency, improved nitrogen utilization, increased carbon assimilation, improved photosynthesis, increased germination power and accelerated maturation.
- Yield can be further influenced by improved plant architecture (under stress and non-stress conditions), including early flowering, control of flowering for hybrid seed production, seedling vigor, plant size, internode count and spacing, root growth, seed size, fruit size , Pod size, pod or ear number, number of seeds per pod or ear, seed mass, increased seed filling, reduced seed drop, reduced pod popping and stability.
- Plants which can be treated according to the invention are hybrid plants which already express the properties of the heterosis or the hybrid effect, which generally leads to higher yield, higher vigor, better health and better resistance to biotic and abiotic stress factors. Such plants are typically produced by crossing an inbred male sterile parental line (the female crossbred partner) with another inbred male fertile parent line (the male crossbred partner). The hybrid seed is typically harvested from the male sterile plants and sold to propagators.
- Pollen sterile plants can sometimes be produced (eg in maize) by delaving (ie mechanical removal of the male reproductive organs or the male flowers); however, it is more common for male sterility to be due to genetic determinants in the plant genome.
- the desired product as one wants to harvest from the hybrid plants, is the seeds, it is usually beneficial to ensure that the pollen fertility in hybrid plants containing the genetic determinants responsible for male sterility , completely restored. This can be achieved by ensuring that the male crossing partners possess appropriate fertility restorer genes capable of restoring pollen fertility in hybrid plants containing the genetic determinants responsible for male sterility. Genetic determinants of pollen sterility may be localized in the cytoplasm.
- CMS cytoplasmic male sterility
- Brassica species examples include Brassica species.
- genetic determinants of pollen sterility may also be localized in the nuclear genome.
- Pollen sterile plants can also be obtained using plant biotechnology methods such as genetic engineering.
- a particularly convenient means of producing male-sterile plants is described in WO 89/10396, wherein, for example, a ribonuclease such as a barnase is selectively expressed in the tapetum cells in the stamens. The fertility can then be restorated by expression of a ribonuclease inhibitor such as barstar in the tapetum cells.
- Plants or plant varieties obtained by methods of plant biotechnology, such as genetic engineering which can be treated according to the invention are herbicide-tolerant plants, i. H. Plants tolerant to one or more given herbicides. Such plants can be obtained either by genetic transformation or by selection of plants containing a mutation conferring such herbicide tolerance.
- Herbicide-tolerant plants are, for example, glyphosate-tolerant plants, ie plants that have been tolerated to the herbicide glyphosate or its salts.
- glyphosate-tolerant plants can be obtained by transforming the plant with a gene encoding the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS).
- EPSPS 5-enolpyruvylshikimate-3-phosphate synthase
- EPSPS 5-enolpyruvylshikimate-3-phosphate synthase
- EPSPS genes are the AroA gene (mutant CT7) of the bacterium Salmonella typhimurium, the CP4 gene of the bacterium Agrobacterium sp., The genes for a EPSPS from the petunia, for a EPSPS from the tomato or for a Encoding EPSPS from Eleusine.
- Glyphosate-tolerant plants can also be obtained by expressing a gene encoding a glyphosate oxidoreductase enzyme. Glyphosate-tolerant plants can also be obtained by expressing a gene that is responsible for a glyphosate acetyltransferase enzyme encoded. Glyphosate-tolerant plants can also be obtained by selecting plants which select naturally occurring mutations of the above mentioned genes.
- herbicidally resistant plants are, for example, plants which have been tolerated against herbicides which inhibit the enzyme glutamine synthase, such as bialaphos, phosphinotricin or glufosinate.
- Such plants can be obtained by expressing an enzyme which detoxifies the herbicide or a mutant of the enzyme glutamine synthase, which is resistant to inhibition.
- an effective detoxifying enzyme is, for example, an enzyme encoding a phosphinotricin acetyltransferase (such as the bar or pat protein from Streptomyces species). Plants expressing an exogenous phosphinotricin acetyltransferase have been described.
- hydroxyphenylpyruvate dioxygenase HPPD
- the hydroxyphenylpyruvate dioxygenases are enzymes that catalyze the reaction in which para-hydroxyphenylpyruvate (HPP) is converted to homogentisate.
- Plants tolerant to HPPD inhibitors can be transformed with a gene encoding a naturally occurring resistant HPPD enzyme or a gene encoding a mutant HPPD enzyme.
- Tolerance to HPPD inhibitors can also be achieved by transforming plants with genes encoding certain enzymes that allow the production of homogentisate despite inhibition of the native HPPD enzyme by the HPPD inhibitor.
- the tolerance of plants to HPPD inhibitors can also be improved by transforming plants with a gene coding for a prephenate dehydrogenase enzyme in addition to a gene which codes for an HPPD-tolerant enzyme.
- ALS inhibitors include sulfonylurea, imidazolinone, triazolopyrimidines, pyrimidinyloxy (thio) benzoates and / or sulfonylaminocarbonyltriazolinone herbicides.
- ALS also known as acetohydroxy acid synthase, AHAS
- AHAS acetohydroxy acid synthase
- plants tolerant to imidazolinone and / or sulfonylurea can be obtained by induced mutagenesis, selection in cell cultures in the presence of the herbicide or by mutation breeding.
- Plants or plant varieties obtained by plant biotechnology methods such as genetic engineering which can also be treated according to the invention are insect-resistant transgenic plants, ie plants which have been made resistant to attack by certain target insects. Such plants can be obtained by genetic transformation or by selection of plants containing a mutation conferring such an insect resistance.
- insect-resistant transgenic plant as used herein includes any plant containing at least one transgene comprising a coding sequence encoding:
- insecticidal crystal protein from Bacillus thuringiensis or an insecticide part thereof, such as the insecticidal crystal proteins found online at:
- a Bacillus thuringiensis crystal protein or a part thereof which is insecticidal in the presence of a second crystal protein other than Bacillus thuringiensis or a part thereof, such as the binary toxin consisting of the crystal proteins Cy34 and Cy35; or
- an insecticidal hybrid protein comprising parts of two different insecticides of Bacillus thuringiensis crystal proteins, such as a hybrid of the proteins of 1) above or a hybrid of the proteins of 2) above, e.g. The protein Cry 1A.105 produced by the corn event MON98034 (WO 2007/027777); or
- VIPs vegetative insecticidal proteins
- a secreted protein from Bacillus thuringiensis or Bacillus cereus which is insecticidal in the presence of a second secreted protein from Bacillus thuringiensis or B. cereus, such as the binary toxin consisting of the proteins VIP 1 A and VTP2A.
- an insecticidal hybrid protein comprising parts of various secreted proteins of Bacillus thuringiensis or Bacillus cereus, such as a hybrid of the proteins of 1) or a hybrid of the proteins of 2) above; or
- 8) a protein according to any one of items 1) to 3) above, in which some, in particular 1 to 10, amino acids have been replaced by another amino acid in order to achieve a higher insecticidal activity against a target insect species and / or the spectrum of the corresponding target insect species and / or due to changes induced in the coding DNA during cloning or transformation (preserving the coding for an insecticidal protein), such as the protein VIP3Aa in cotton event COT 102.
- insect-resistant transgenic plants in the present context also include any plant comprising a combination of genes encoding the proteins of any of the above classes 1 to 8.
- an insect resistant plant contains more than one transgene encoding a protein of any one of the above 1 to 8 in order to enhance the spectrum of the corresponding target insect species. or to delay the development of resistance of the insects to the plants by using various proteins that are insecticidal to the same species of target insects, but have a different mode of action, such as binding to different receptor binding sites in the insect.
- Plants or plant varieties obtained by methods of plant biotechnology, such as genetic engineering), which can also be treated according to the invention, are tolerant of abiotic stress factors. Such plants can be obtained by genetic transformation or by selection of plants containing a mutation conferring such stress resistance. Particularly useful plants with stress tolerance include the following:
- Plants which contain a transgene capable of reducing the expression and / or activity of the gene for the poly (ADP-ribose) polymerase (PARP) in the plant cells or plants.
- PARP poly (ADP-ribose) polymerase
- Plants which contain a stress tolerance-enhancing transgene encoding a plant-functional enzyme of the nicotinamide adenine dinucleotide salvage biosynthetic pathway including nicotinamidase, nicotinate phosphoribosyltransferase, nicotinic acid mononucleotide adenyltransferase, nicotinamide adenine dinucleotide synthetase or nicotinamide phosphoribosyltransferase.
- Plants or plant varieties obtained by plant biotechnology methods such as genetic engineering, which can also be treated according to the invention, have an altered quantity, quality and / or shelf life of the harvested product and / or altered properties of certain components of the harvested product on, such as:
- Transgenic plants which synthesize a modified starch with respect to their physicochemical properties, in particular amylose content or amylose / amylopectin ratio, degree of branching, average chain length, side chain distribution, viscosity behavior, gel strength, starch grain size and / or starch comorphology as compared to the synthesized starch in wild-type plant cells or plants, so that this modified starch is better suited for certain applications.
- Transgenic plants that synthesize non-starch carbohydrate polymers or non-starch carbohydrate polymers whose properties are altered compared to wild-type plants without genetic modification. Examples are plants that produce polyfructose, particularly of the inulin and levan type, plants that produce alpha-1,4-glucans, plants that produce alpha-1,6-branched alpha-1,4-glucans, and plants that produce Produce alternan.
- Plants or plant cultivars obtained by plant biotechnology methods such as genetic engineering, which can also be treated according to the invention, are plants such as cotton plants with altered fiber properties. Such plants can be through genetic transformation or through Selection of plants containing a mutation conferring such altered fiber properties; these include:
- plants such as cotton plants, containing an altered form of cellulose synthase genes
- plants such as cotton plants, containing an altered form of rsw2 or rsw3 homologous nucleic acids
- plants such as cotton plants having increased expression of sucrose phosphate synthase
- plants such as cotton plants with increased expression of sucrose synthase
- plants such as cotton plants with modified reactivity fibers, e.g. By expression of the N-acetylglucosamine transferase gene, including nodC, and chitin synthase genes.
- Plants or plant varieties obtained by plant biotechnology methods such as genetic engineering which can also be treated according to the invention are plants such as oilseed rape or related Brassica plants with altered oil composition properties. Such plants can be obtained by genetic transformation or by selection of plants containing a mutation conferring such altered oil properties; these include:
- plants such as oilseed rape plants, which produce oil of high oleic acid content
- plants such as oilseed rape plants, which produce oil with a low linolenic acid content.
- transgenic plants such as rape plants that produce oil with a low saturated fatty acid content.
- Particularly useful transgenic plants which can be treated according to the invention are plants with one or more genes coding for one or more toxins, the transgenic plants offered under the following commercial names: YIELD GARD® (for example maize, cotton, Soybeans), KnockOut® (for example corn), BiteGard® (for example maize), BT-Xtra® (for example corn), StarLink® (for example maize), Bollgard® (cotton), Nucotn® (cotton), Nucotn 33B® (cotton), NatureGard® (for example corn), Protecta® and NewLeaf® (potato).
- YIELD GARD® for example maize, cotton, Soybeans
- KnockOut® for example corn
- BiteGard® for example maize
- BT-Xtra® for example corn
- StarLink® for example maize
- Bollgard® cotton
- Nucotn® cotton
- Herbicide-tolerant crops to be mentioned are, for example, corn, cotton and soybean varieties sold under the following tradenames: Roundup Ready® (glyphosate tolerance, for example corn, cotton, soybean), Liberty Link® (phosphinotricin tolerance, for example rapeseed) , ⁇ ® (imidazolinone tolerance) and SCS® (sylphonylurea tolerance), for example maize.
- Herbicide-resistant plants (plants traditionally grown for herbicide tolerance) to be mentioned include the varieties sold under the name Clearfield® (for example corn).
- transgenic plants that can be treated according to the invention are plants that contain transformation events, or a combination of transformation events, and that are listed, for example, in the files of various national or regional authorities (see, for example, http : //gmoinfo.jrc.it/gmp_browse.aspx and http://www.agbios.com/dbase.php).
- the active compounds or compositions according to the invention can also be used in the protection of materials for the protection of industrial materials against infestation and destruction by undesired microorganisms, such as fungi.
- Technical materials as used herein mean non-living materials that have been prepared for use in the art.
- technical materials to be protected from fungal change or destruction by the active compounds of the present invention may be adhesives, glues, paper, wallboard and board, textiles, carpets, leather, wood, paints and plastics, coolants, and other microorganism-infested materials or can be decomposed.
- parts of production plants and buildings e.g. Cooling water circuits, cooling and heating systems and ventilation and air conditioning systems, which may be affected by the proliferation of microorganisms.
- technical materials which may be mentioned are preferably adhesives, glues, papers and cartons, leather, wood, paints, cooling lubricants and heat transfer fluids, particularly preferably wood.
- the active compounds or compositions according to the invention can prevent adverse effects such as vermouth, deterioration, decomposition, discoloration or mold.
- the compounds of the invention for protection against fouling of objects in particular of hulls, screens, nets, structures, quays and signal systems, which come in contact with seawater or brackish water, can be used.
- the inventive method for controlling unwanted fungi can also be used for the protection of so-called storage goods.
- Storage goods of plant origin such as plants or plant parts, such as stems, leaves, tubers, seeds , Fruits, grains, can be protected in freshly harvested condition or after processing by (pre-) drying, moistening, crushing, grinding, pressing or roasting.
- Storage Goods also includes timber, whether unprocessed, such as lumber, power poles and barriers, or in the form of finished products, such as furniture, storage goods of animal origin are, for example, skins, leather, furs and hair.
- the active compounds according to the invention can prevent disadvantageous effects such as decay, deterioration, disintegration, discoloration or mold.
- Bremia species such as, for example, Bremia lactucae
- Peronospora species such as Peronospora pisi or P. brassicae
- Phytophthora species such as Phytophthora infestans
- Plasmopara species such as Plasmoparavicola
- Pseudoperonospora species such as, for example, Pseudoperonospora humuli or Pseudoperonospora cubensis
- Pythium species such as Pythium ultimum
- Phaeosphaeria species such as Phaeosphaeria nodorum
- Pyrenophora species such as, for example, Pyrenophora teres
- Ramularia species such as Ramularia collo-cygni
- Rhynchosporium species such as, for example, Rhynchosporium secalis
- Septoria species such as Septoria apii
- Typhula species such as Typhula incarnata
- Venturia species such as Venturia inaequales
- Ear and panicle diseases caused by e.g. Alternaria species, such as Alternaria spp .; Aspergillus species, such as Aspergillus flavus; Cladosporium species, such as Cladosporium cladosporioides; Claviceps species, such as Claviceps purpurea; Fusarium species such as Fusarium culmorum; Gibberella species, such as Gibberella zeae; Monographella species, such as Monographella nivalis; Septoria species such as Septoria nodorum;
- Alternaria species such as Alternaria spp .
- Aspergillus species such as Aspergillus flavus
- Cladosporium species such as Cladosporium cladosporioides
- Claviceps species such as Claviceps purpurea
- Fusarium species such as Fusarium culmorum
- Gibberella species such as Gibberella
- Sphacelotheca species such as Sphace- lotheca reiliana
- Tilletia species such as Tilletia caries, T. controversa
- Uro cystis species such as Urocystis occulta
- Ustilago species such as Ustilago nuda, U. nuda tritici
- Botrytis species such as Botrytis cinerea
- Penicillium species such as Penicillium expansum and P. purpurogenum
- Sclerotinia species such as Sclerotinia sclerotiorum
- Sphacelotheca species such as Sphace- lotheca reiliana
- Tilletia species such as Tilletia caries, T. controversa
- Uro cystis species such as Urocystis occulta
- Ustilago species such as Ustilago nuda,
- Verticilium species such as Verticilium alboatrum
- Nectria species such as Nectria galligena
- Botrytis species such as Botrytis cinerea
- Diseases of plant tubers caused by e.g. Rhizoctonia species, such as Rhizoctonia solani
- Helminthosporium species such as Helminthosporium solani
- Xanthomonas species such as Xanthomonas campestris pv. Oryzae
- Pseudomonas species such as Pseudomonas syringae pv. Lachrymans
- Erwinia species such as Erwinia amylovora.
- the following diseases of soybean beans can be controlled:
- Phytophthora red (Phytophthora megasperma), Brown Stem Red (Phialophora gregata), Pythium red (Pythium aphanidermatum, Pythium irregular, Pythium debaryanum, Pythium myriotylum, Pythium ultimum) , Rhizoctonia Root Red, Stem Decay, and Damping Off (Rhizoctonia solani), Sclerotinia Stem Decay (Sclerotinia sclerotiorum), Sclerotinia Southern Blight (Sclerotinia rolfsii), Thielaviopsis Root Red (Thielaviopsis basicola).
- the active compounds according to the invention preferably act against fungi, in particular molds, wood-discolouring and wood-destroying fungi (Basidiomycetes).
- fungi in particular molds, wood-discolouring and wood-destroying fungi (Basidiomycetes).
- Basidiomycetes fungi of the following genera: Alternaria, such as Alternaria tenuis; Aspergillus, such as Aspergillus niger; Chaetomium, like Chaetomium globosum; Coniophora, like Coniophora puetana; Lentinus, like Lentinus tigrinus; Penicillium, like Penicillium glaucum; Polyporus, such as Polyporus versicolor; Aureobasidium, such as Aureobasidium pullulans; Sclerophoma, such as Sclerophomapityophila; Trichoderma, like Trichoderma viride.
- the active compounds according to the invention also have very good antifungal effects. They have a very broad antimycotic spectrum of activity, in particular against dermatophytes and yeasts, mold and diphasic fungi (eg against Candida species such as Candida albicans, Candida glabrata) and Epidermophyton floccosum, Aspergillus species such as Aspergillus niger and Aspergillus fumigatus, Trichophyton Species such as Trichophyton mentagrophytes, Microsporon species such as Microsporon canis and audouinii.
- the list of these fungi is by no means a limitation of the detectable mycotic spectrum, but has only an explanatory character.
- the application rates can be varied within a relatively wide range, depending on the mode of administration.
- the application rate of the active compounds according to the invention is
- Leaves from 0.1 to 10,000 g / ha, preferably from 10 to 1,000 g / ha, more preferably from 50 to 300 g / ha (when applied by pouring or dropping, the rate of application can even be reduced, especially if inert substrates such as rockwool or perlite are used);
- seed treatment from 2 to 200 g per 100 kg of seed, preferably from 3 to 150 g per 100 kg of seed, more preferably from 2.5 to 25 g per 100 kg of seed, most preferably from 2.5 to 12.5 g per 100 kg of seed;
- the active compounds or compositions according to the invention can therefore be used to protect plants within a certain period of time after the treatment against attack by the mentioned pathogens.
- the period within which protection is induced generally extends to 1 to 28 days, preferably to 1 to 14 days, more preferably to 1 to 10 days, most preferably to 1 to 7 days after the treatment of the plants the active substances or up to 200 days after seed treatment.
- the treatment according to the invention can be reduced by the treatment according to the invention, the mycotoxin content in the crop and the food and feed produced therefrom.
- mycotoxins include: deoxynivalenol (DON), nivalenol, 15-Ac-DON, 3-Ac-DON, T2 and HT2 toxin, fumonisins, zearalenone, moniliformin, fusarin, diaceotoxyscirpenol (DAS) , Beauvericin, enniatine, fusaroproliferin, fusarenol, ochratoxins, patulin, ergot alkaloids and aflatoxins, which may be caused, for example, by the following fungi: Fusarium spec., Such as Fusarium acuminatum, F. avenaceum, F.
- DON deoxynivalenol
- 15-Ac-DON 15-Ac-DON
- 3-Ac-DON 3-Ac-DON
- T2 and HT2 toxin fumonisins
- zearalenone moniliformin
- Example A Alternaria test (tomato) / protective
- Emulsifier 1 part by weight of alkylaryl polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- young tomato plants are sprayed with the preparation of active compound in the stated application rate.
- the plants are inoculated with a spore suspension of Alternaria solani and then stand for 24 h at 100% rel. Humidity and 22 ° C.
- the plants are at 96% rel. Humidity and a temperature of 20 ° C. 7 days after the inoculation the evaluation takes place.
- 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed.
- the following compounds according to the invention show an efficiency of 70% or more at a concentration of active ingredient of 500 ppm.
- Emulsifier 1 part by weight of alkylaryl polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- young tomato plants are sprayed with the preparation of active compound in the stated application rate.
- the plants are inoculated with a spore suspension of Phytophthora infestans and then stand for 24 h at 100% rel. Humidity and 22 ° C.
- the plants are placed in a climate cell at about 96% relative humidity and a temperature of about 20 ° C. 7 days after the inoculation the evaluation takes place.
- 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed becomes.
- the following compounds according to the invention show an efficacy of 70% or more at a concentration of active ingredient of 500 ppm.
- Table B Phytophthora test (tomato) / protective
- Example C Plasmopara test (vine) / protective
- Emulsifier 1 part by weight of alkyl-aryl-polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- young plants are sprayed with the preparation of active compound in the stated application rate. After the spray coating has dried on, the plants are inoculated with an aqueous spore suspension of Plasmopara viticola and then left for 1 day in an incubation booth at about 20 ° C. and 100% relative atmospheric humidity. Subsequently, the plants are placed in the greenhouse for 4 days at about 21 ° C and about 90% humidity. The plants are then moistened and placed in an incubation cabin for 1 day. 6 days after the inoculation the evaluation takes place.
- Example D Venturia test (apple) / protective
- Emulsifier 1 part by weight of alkyl-aryl-polyglycol ether
- a suitable preparation of active compound 1 part by weight of active compound is mixed with the indicated amounts of solvent and emulsifier, and the concentrate is diluted with water to the desired concentration.
- young plants are sprayed with the preparation of active compound in the stated application rate. After the spray coating has dried on, the plants are inoculated with an aqueous conidia suspension of the apple scab pathogen Venturia inaequalis and then remain in an incubation cabin for 1 day at about 20 ° C. and 100% relative atmospheric humidity. The plants are then placed in the greenhouse at about 21 ° C and a relative humidity of about 90%. 10 days after the inoculation the evaluation takes place. In this case, 0% means an efficiency which corresponds to that of the control, while an efficiency of 100% means that no infestation is observed. In this test, the following compounds of the invention show an efficiency of 70% or more at a concentration of active ingredient of 100 ppm.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2796156A CA2796156A1 (en) | 2010-04-14 | 2011-04-11 | Thienodithiin derivatives as fungicides |
EP11713788.5A EP2558471B1 (de) | 2010-04-14 | 2011-04-11 | Thienodithiinderivate als Fungizide |
CN201180029562.3A CN102939293B (zh) | 2010-04-14 | 2011-04-11 | 作为杀菌剂的噻吩并二噻英衍生物 |
KR1020127029245A KR20140046967A (ko) | 2010-04-14 | 2011-04-11 | 살진균제로서의 티에노디티인 유도체 |
ES11713788.5T ES2483132T3 (es) | 2010-04-14 | 2011-04-11 | Derivados de tienoditiina como fungicidas |
BR112012026150A BR112012026150A2 (pt) | 2010-04-14 | 2011-04-11 | derivados de tienodititina. |
MX2012011783A MX2012011783A (es) | 2010-04-14 | 2011-04-11 | Derivados de tienoditiina. |
JP2013504223A JP5746752B2 (ja) | 2010-04-14 | 2011-04-11 | 殺菌剤としてのチエノジチイン誘導体 |
Applications Claiming Priority (4)
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EP10159901 | 2010-04-14 | ||
EP10159901.7 | 2010-04-14 | ||
US32506510P | 2010-04-16 | 2010-04-16 | |
US61/325,065 | 2010-04-16 |
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PCT/EP2011/055635 WO2011128295A1 (de) | 2010-04-14 | 2011-04-11 | Thienodithiinderivate als fungizide |
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US (1) | US8383551B2 (de) |
EP (1) | EP2558471B1 (de) |
JP (1) | JP5746752B2 (de) |
KR (1) | KR20140046967A (de) |
CN (1) | CN102939293B (de) |
AR (1) | AR081532A1 (de) |
BR (1) | BR112012026150A2 (de) |
CA (1) | CA2796156A1 (de) |
CO (1) | CO6630138A2 (de) |
CR (1) | CR20120520A (de) |
ES (1) | ES2483132T3 (de) |
GT (1) | GT201200278A (de) |
MX (1) | MX2012011783A (de) |
TW (1) | TWI488580B (de) |
WO (1) | WO2011128295A1 (de) |
Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3364229A (en) * | 1964-01-30 | 1968-01-16 | Shell Oil Co | 1, 4 dithiin-2, 3, 5, 6-tetracarboximides and process for their preparation |
JPS4811020B1 (de) * | 1970-09-28 | 1973-04-10 | ||
JPS5040736A (de) * | 1973-08-09 | 1975-04-14 | ||
US4245432A (en) | 1979-07-25 | 1981-01-20 | Eastman Kodak Company | Seed coatings |
US4272417A (en) | 1979-05-22 | 1981-06-09 | Cargill, Incorporated | Stable protective seed coating |
US4808430A (en) | 1987-02-27 | 1989-02-28 | Yazaki Corporation | Method of applying gel coating to plant seeds |
WO1989010396A1 (en) | 1988-04-28 | 1989-11-02 | Plant Genetic Systems N.V. | Plants with modified stamen cells |
WO1996019481A1 (en) * | 1994-12-21 | 1996-06-27 | The Dow Chemical Company | Dimercapto-1,3-dithiolo-2-one or thione maleimides, compositions containing them and their use as antimicrobial and marine antifouling agents |
WO1996033270A1 (en) | 1995-04-20 | 1996-10-24 | American Cyanamid Company | Structure-based designed herbicide resistant products |
US5876739A (en) | 1996-06-13 | 1999-03-02 | Novartis Ag | Insecticidal seed coating |
WO2002028186A2 (en) | 2000-10-06 | 2002-04-11 | Monsanto Technology, Llc | Seed treatment with combinations of insecticides |
WO2002080675A1 (en) | 2001-03-21 | 2002-10-17 | Monsanto Technology, Llc | Treated plant seeds with controlled release of active agents |
US20030176428A1 (en) | 1998-11-16 | 2003-09-18 | Schneidersmann Ferdinand Martin | Pesticidal composition for seed treatment |
WO2007024782A2 (en) | 2005-08-24 | 2007-03-01 | Pioneer Hi-Bred International, Inc. | Compositions providing tolerance to multiple herbicides and methods of use thereof |
WO2007027777A2 (en) | 2005-08-31 | 2007-03-08 | Monsanto Technology Llc | Nucleotide sequences encoding insecticidal proteins |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0811020B2 (ja) * | 1990-08-10 | 1996-02-07 | ホクト産業株式会社 | きのこ栽培用コンテナ |
CN100349516C (zh) * | 2003-06-26 | 2007-11-21 | 巴斯福股份公司 | 杀真菌混合物 |
-
2011
- 2011-04-11 WO PCT/EP2011/055635 patent/WO2011128295A1/de active Application Filing
- 2011-04-11 EP EP11713788.5A patent/EP2558471B1/de not_active Not-in-force
- 2011-04-11 JP JP2013504223A patent/JP5746752B2/ja not_active Expired - Fee Related
- 2011-04-11 CN CN201180029562.3A patent/CN102939293B/zh not_active Expired - Fee Related
- 2011-04-11 ES ES11713788.5T patent/ES2483132T3/es active Active
- 2011-04-11 CA CA2796156A patent/CA2796156A1/en not_active Abandoned
- 2011-04-11 KR KR1020127029245A patent/KR20140046967A/ko not_active Application Discontinuation
- 2011-04-11 MX MX2012011783A patent/MX2012011783A/es active IP Right Grant
- 2011-04-11 BR BR112012026150A patent/BR112012026150A2/pt not_active Application Discontinuation
- 2011-04-12 TW TW100112536A patent/TWI488580B/zh not_active IP Right Cessation
- 2011-04-13 AR ARP110101245A patent/AR081532A1/es not_active Application Discontinuation
- 2011-04-14 US US13/087,213 patent/US8383551B2/en not_active Expired - Fee Related
-
2012
- 2012-10-11 GT GT201200278A patent/GT201200278A/es unknown
- 2012-10-12 CO CO12181003A patent/CO6630138A2/es active IP Right Grant
- 2012-10-12 CR CR20120520A patent/CR20120520A/es unknown
Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3364229A (en) * | 1964-01-30 | 1968-01-16 | Shell Oil Co | 1, 4 dithiin-2, 3, 5, 6-tetracarboximides and process for their preparation |
JPS4811020B1 (de) * | 1970-09-28 | 1973-04-10 | ||
JPS5040736A (de) * | 1973-08-09 | 1975-04-14 | ||
US4272417A (en) | 1979-05-22 | 1981-06-09 | Cargill, Incorporated | Stable protective seed coating |
US4245432A (en) | 1979-07-25 | 1981-01-20 | Eastman Kodak Company | Seed coatings |
US4808430A (en) | 1987-02-27 | 1989-02-28 | Yazaki Corporation | Method of applying gel coating to plant seeds |
WO1989010396A1 (en) | 1988-04-28 | 1989-11-02 | Plant Genetic Systems N.V. | Plants with modified stamen cells |
WO1996019481A1 (en) * | 1994-12-21 | 1996-06-27 | The Dow Chemical Company | Dimercapto-1,3-dithiolo-2-one or thione maleimides, compositions containing them and their use as antimicrobial and marine antifouling agents |
WO1996033270A1 (en) | 1995-04-20 | 1996-10-24 | American Cyanamid Company | Structure-based designed herbicide resistant products |
US5876739A (en) | 1996-06-13 | 1999-03-02 | Novartis Ag | Insecticidal seed coating |
US20030176428A1 (en) | 1998-11-16 | 2003-09-18 | Schneidersmann Ferdinand Martin | Pesticidal composition for seed treatment |
WO2002028186A2 (en) | 2000-10-06 | 2002-04-11 | Monsanto Technology, Llc | Seed treatment with combinations of insecticides |
WO2002080675A1 (en) | 2001-03-21 | 2002-10-17 | Monsanto Technology, Llc | Treated plant seeds with controlled release of active agents |
WO2007024782A2 (en) | 2005-08-24 | 2007-03-01 | Pioneer Hi-Bred International, Inc. | Compositions providing tolerance to multiple herbicides and methods of use thereof |
WO2007027777A2 (en) | 2005-08-31 | 2007-03-08 | Monsanto Technology Llc | Nucleotide sequences encoding insecticidal proteins |
Non-Patent Citations (4)
Title |
---|
L. D. S. YADAV ET AL.: "Synthesis and fungitoxicity of rationally designed thiazolo-1,3-dithiins, -thiazines, and -oxathiinsa", J. AGRIC. FOOD CHEM., vol. 40, no. 7, 1992, pages 1214 - 1216, XP002586442 * |
R. WEGLER: "Chemie der Pflanzenschutz-und Schädlingsbekämpfungsmittel", vol. 2, 1970, SPRINGER VERLAG, pages: 401 - 412 |
RAJAB ABU-EL-HALAWA ET AL: "Synthesis of Novel N-Substituted 6-Chlorothieno-(2,3-e)-1,4,2-Dithiaz in-3-Amine 1,1-Dioxides", HETEROCYCLES, ELSEVIER SCIENCE PUBLISHERS B.V. AMSTERDAM, NL, vol. 75, no. 7, 1 July 2008 (2008-07-01), pages 1749 - 1755, XP009134640, ISSN: 0385-5414, [retrieved on 20080226] * |
S. A. AMELICHEV ET AL.: "Synthesis of 1,4-Dithiins from Pentathiepins", ORGANIC LETTERS, vol. 8, no. 20, 2006, pages 4529 - 4532, XP002586441 * |
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CA2796156A1 (en) | 2011-10-20 |
JP5746752B2 (ja) | 2015-07-08 |
MX2012011783A (es) | 2012-11-22 |
CO6630138A2 (es) | 2013-03-01 |
CN102939293A (zh) | 2013-02-20 |
US20110281915A1 (en) | 2011-11-17 |
GT201200278A (es) | 2014-01-27 |
TW201204259A (en) | 2012-02-01 |
EP2558471A1 (de) | 2013-02-20 |
CN102939293B (zh) | 2014-10-01 |
AR081532A1 (es) | 2012-10-03 |
JP2013523855A (ja) | 2013-06-17 |
TWI488580B (zh) | 2015-06-21 |
EP2558471B1 (de) | 2014-05-21 |
US8383551B2 (en) | 2013-02-26 |
CR20120520A (es) | 2013-03-08 |
ES2483132T3 (es) | 2014-08-05 |
KR20140046967A (ko) | 2014-04-21 |
BR112012026150A2 (pt) | 2015-09-08 |
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